| Literature DB >> 32275863 |
Xi Zhang1, Daqi Yu2, Jingchuan Sun3, Yujie Wu3, Junyuan Gong4, Xuemei Li5, Li Liu4, Shan Liu4, Jianbo Liu3, Yulan Wu4, Dongyang Li4, Yinping Ma6, Xu Han2, Yanan Zhu2, Zhaolong Wu2, Yihua Wang2, Qi Ouyang7, Tao Wang8.
Abstract
Tyrosine kinase receptor of insulin-like growth factor 1 receptor (IGF-1R) and insulin receptor (IR) bind to hormones, such as insulin, IGF-1, and IGF-2, and transduces the signals across the cell membrane. However, the complete structure of the receptor and the signal transduction mechanism remains unclear. Here, we report the cryo-EM structure of the ligand-bound ectodomain in the full-length human IGF-1R. We reconstructed the IGF-1R/insulin complex at 4.7 Å and the IGF-1R/IGF-1 complex at 7.7 Å. Our structures reveal that only one insulin or one IGF-1 molecule binds to and activates the full-length human IGF-1R receptor.Entities:
Keywords: IGF-1; IGF-1r; cryo-EM; insulin
Mesh:
Substances:
Year: 2020 PMID: 32275863 DOI: 10.1016/j.str.2020.03.007
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006